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FDA Grants 510(k) Clearance to ABANZA's WasherCap™ Mini for Meniscal Root Repair and ACL Reconstruction

5 months ago3 min read

Key Insights

  • ABANZA has received FDA 510(k) clearance for its WasherCap™ Mini fixation system, the first knotless, bidirectionally tension-adjustable device for meniscal root repair and ACL reconstruction.

  • Biomechanical testing demonstrates the WasherCap™ Mini provides superior fixation strength and minimal displacement during cyclic loading compared to conventional devices like cortical buttons and suture anchors.

  • The device addresses a growing market of nearly 100,000 meniscal root repair procedures annually in the US, with potential to improve outcomes and slow arthritis progression through precise anatomical restoration.

ABANZA announced today that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for its innovative WasherCap™ Mini fixation system, designed for meniscal root repair and ACL reconstruction procedures. This breakthrough device represents a significant advancement in orthopedic soft tissue repair technology.
The WasherCap™ Mini is the first suture and tape fixation device to offer surgeons a knotless, bidirectionally tension-adjustable solution that functions effectively regardless of bone quality. This unique capability addresses a critical need in sports medicine procedures where precise tension control directly impacts surgical outcomes.

Superior Biomechanical Performance

Rigorous testing has demonstrated that the WasherCap™ Mini delivers superior fixation strength compared to conventional devices currently used in orthopedic procedures. The device showed minimal displacement during cyclic loading tests when compared to traditional alternatives such as cortical buttons and suture anchors.
These performance characteristics are particularly important for procedures requiring long-term stability of the repair, as inadequate fixation can lead to repair failure and poor clinical outcomes.

Addressing a Growing Clinical Need

Meniscal root repair represents one of the fastest-growing segments in sports medicine, with approximately 100,000 procedures performed annually in the United States alone. The meniscus plays a crucial role in knee joint biomechanics, and root tears can significantly compromise its function.
As the first FDA-cleared knotless and bidirectionally tension-adjustable fixation system specifically designed for meniscal root repair, the WasherCap™ Mini offers surgeons unprecedented control during these technically demanding procedures.
"FDA clearance of the WasherCap™ Mini is a tremendous milestone for ABANZA," said Juan Abascal, Chief Executive Officer at ABANZA. "Our device provides surgeons with a highly reliable solution for suture and tape fixation—particularly in surgeries where precise tension control is critical."
Abascal emphasized the clinical significance of the technology: "For meniscal root repair, its knotless technology corrects extrusion and restores the meniscus to its anatomical position, which we believe will lead to better short and long-term outcomes, while potentially slowing the progression of arthritis."

Expanding Innovation Portfolio

The WasherCap™ Mini represents the second device in ABANZA's growing platform of products built on disruptive fixation technology. The company has announced plans to expand its portfolio with upcoming innovations including the WasherCap™ In Line and the LoopCap™.
These forthcoming devices will target additional orthopedic applications including biceps tenodesis, medial collateral ligament repairs, and complex foot and ankle pathologies, further extending ABANZA's reach in the soft tissue repair market.

Clinical Implications

The introduction of the WasherCap™ Mini could significantly impact clinical practice in sports medicine. Traditional meniscal root repair techniques often involve complex knot-tying procedures that can be technically challenging and may result in variable tension across the repair.
By offering a knotless solution with bidirectional tension adjustment, the WasherCap™ Mini may help standardize the procedure while potentially improving anatomical restoration of the meniscus. This precise positioning is critical for restoring normal knee biomechanics and potentially limiting the progression of degenerative changes in the joint.
For ACL reconstruction procedures, the device offers similar advantages in providing stable fixation with optimal tension control, which is essential for successful graft integration and long-term function.
The technology's ability to perform consistently regardless of bone quality also addresses an important clinical challenge, as variable bone density can compromise the effectiveness of traditional fixation methods, particularly in older patients or those with compromised bone quality.
With this FDA clearance, ABANZA continues to advance its mission of revolutionizing orthopedic and arthroscopic soft tissue repair through innovative medical devices designed to enhance patient outcomes and improve quality of life.
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